Effects of rapamycin-loaded poly(lactic-co-glycolic) acid nanoparticles on distribution of cell cycle, expression of p27 protein, and proliferation of human umbilical arterial vascular smooth muscle cell in vitro.
- VernacularTitle:雷帕霉素聚乳酸-聚乙醇酸共聚物纳米粒子对人脐动脉平滑肌细胞细胞周期时相、p27蛋白表达及细胞增殖的影响
- Author:
Li-fu MIAO
1
;
Chao-lian HUANG
;
Lian-feng CHEN
;
Wen-ling ZHU
;
Jing YANG
;
Yi-guang WANG
;
Hua ZHANG
;
Pei-mao LIU
;
Ming-peng SHE
;
Cun-xian SONG
Author Information
- Publication Type:Journal Article
- MeSH: Cell Cycle; drug effects; Cell Proliferation; drug effects; Cells, Cultured; Cyclin-Dependent Kinase Inhibitor p27; metabolism; Drug Carriers; Humans; Lactic Acid; Muscle, Smooth, Vascular; cytology; Myocytes, Smooth Muscle; cytology; drug effects; metabolism; Nanoparticles; Polyglycolic Acid; Sirolimus; administration & dosage; pharmacology; Umbilical Arteries; cytology
- From: Acta Academiae Medicinae Sinicae 2010;32(1):32-38
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the effects of rapamycin (RPM)-loaded poly (lactic-co- glycolic) acid (PLGA) nanoparticles (NPs) on the proliferation, distribution of cell cycle, and expression of p27 protein in human umbilical arterial vascular smooth muscle cell (HUASMC) in vitro.
METHODSThe primarily culture model of HUASMC was successfully established by explant-attached method in vitro. The cells were administrated with different doses of RPM, and RPM-PLGA NPs were observed as treat groups compared with PLGA NPs and M231-SMGs medium cultured group. The effect of RPM-PLGA NPs on proliferation of HUASMC was assessed using 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) colorimetry method. The influences of RPM-PLGA NPs on the cell cycle and cellular growth kinetics of HUASMCs were tested by flow cytometry. The effect of RPM-PLGA NPs on the expression of p27 protein of HUASMCs was assessed through an immunohistochemical method.
RESULTSCompared with the control group, the proliferation of HUASMCs was inhibited by 50 microg/L and higher concentration of RPM-PLGA NPs in a dose-dependent manner (P < 0.05). The numbers of cells entering cell cycle of S/G2/M phases were significantly lower in RPM-PLGA NPs and RPM treated groups. Histologically, the expression of p27 were up-regulated in 500 microg/L RPM-PLGA NPs and 100 microg/L RPM treated group (all P < 0.01 ) when compared with the control group.
CONCLUSIONSRPM-PLGA NPs has a similar effects as RPM in inhibiting the growth of in vitro cultured HUASMC. It can remarkably suppress the expression of in vitro cultured HUASMC p27 protein, arrest its cell cycle at G1/S phase, and inhibit its proliferation.
